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WorldTraining

Essentials of Dealing with Non-Conforming Material


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Who should attend?

Quality Systems Specialists Document Control Specialists Quality and Compliance Specialists Internal Auditors and Managers Quality Engineers Manufacturing Managers CAPA Specialists

Details

Overview:
You'll learn how to identify, segregate, control, and disposition non-conforming material. You'll learn about conducting failure investigations and requirements for correction and corrective action.

Why should you Attend:
Dealing with non-conforming material is a necessary process for medical device manufacturers. Yet, non-conforming material is a top reason for 483 and Warning letter citations.

Areas Covered in the Session:
Overview of the Regulations
Definitions and Expectations
Segregation and Control
Disposition of NC material
Concessions

Who Will Benefit:
Quality Systems Specialists
Document Control Specialists
Quality and Compliance Specialists
Internal Auditors and Managers
Quality Engineers

Speaker Profile:
Susanne Manz MBA, MBB, RAC, CQA is an accomplished leader in the medical device industry with emphasis on quality, compliance, and six sigma. She has an extensive background in quality and compliance for medical devices from new product development, to operations, to post-market activities.

Event Fee: One Dial-in One Attendee Price: US$150.00

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com

Prices

One Dial-in One Attendee Price: $150.00

Contact

Event Manager
support@compliance4all.com

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